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Front Cover: Palladium Catalyzed Direct Acylation of Iodo‐Acetanilides/Iodo‐Phenyl Acetates: Domino One‐Pot Synthesis of 2‐Quinolinones (Eur. J. Org. Chem. 8/2018)
Author(s) -
Basuli Scuhand,
Satyanarayana Gedu
Publication year - 2018
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201800172
Subject(s) - chemistry , acetanilide , domino , acylation , palladium , catalysis , cascade reaction , combinatorial chemistry , hydrolysis , one pot synthesis , organic chemistry
The Front Cover shows a domino directing group free one‐pot synthesis of 2‐quinolinones from ortho ‐iodoacetanilides by palladium catalyzed direct acylation as the key step. The background represents a water source, signifying that the reaction is water tolerant and water in the TBHP helped to promote the reaction. Non‐toxic aldehydes are used as acylating agents instead of toxic CO gas. In addition, one‐pot formation of ortho ‐acylanilines via in situ base hydrolysis of ortho ‐iodoacetanilides is also presented. Significantly, the strategy was extended to the domino one‐pot synthesis of drugs and bioactive compounds, for example, the syntheses of an HBV inhibitor and a key intermediate of Tipifarnib. More information can be found in the Full Paper by S. Basuli and G. Satyanarayana .